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FDA
Food and Drug Administration · Recall Z-2563-2026 · Apr 30, 2026

Surgify Halo, 40 mm, Long, Model/Catalog Number: 40.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY

The hazard

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

Surgify Halo, 40 mm, Long, Model/Catalog Number: 40.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered)

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model UDI: 06429811532274Model All lots until the IFU update has been implementedUPC 06429811532274

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.